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Incidentaloma physical examination

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mohammed Abdelwahed M.D[2]

Overview

Most of patients will not show any special signs as the definition of adrenal incidentaloma means incidentaly discovered mass during imaging for ant other reasons. Some cases show signs of subclinical Cushing’s syndrome, pheochromocytoma, or hyperaldosteronism. Common physical examination findings of include patients may appear quite well if the disease is asymptomatic. Patients may appear tired, weak, diaphoretic and anxious. Tachypnea if malignant secondaries are found in the lung with a rapid strong equal pulse and high blood pressure. Jaundice, hyperpigmentation, Telangiectasia, thinning of the skin and easy bruising may be found. A palpable abdominal mass in the lower abdominal quadrant may be found. Hyporeflexia due to low potassium level in aldosternonma, Proximal muscle weakness bilaterally, and bilateral tremors may be found.

Incidentaloma physical examination

Physical examination of incidentaloma is dependent on the underlying cause and the nature of the lesion in the adrenal glands. Some cases may show signs of subclinical Cushing’s syndrome, pheochromocytoma, or hyperaldosteronism.

Physical Examination of subclinical Cushing’s syndrome

Physical examination of patients with subclinical Cushing’s syndrome is as follows:[1]

Appearance of the patient

  • Patients with Cushing’s syndrome usually appears overweight.

Vital signs

  • Moon-face is a medical sign where the face swells up into a rounded shape. It is often associated with Cushing’s syndrome, which has led to it being known as Cushingoid facies (“Cushings-like face”), or steroid treatment, which has led to the name steroid facies.

Skin

Eye

Neck

  • Growth of fat pads along the collar bone and on the back of the neck (known as a lipodystrophy)
Features of Cushing’s syndrome(Image courtesy of Jessica Stevenson, and http://www.physio-pedia.com/File:Cushings-syndrome2.jpg#filelinks)

Physical Examination of pheochromocytoma

Appearance of the Patient

Vital Signs

Skin

Head

Neck

Lungs

Heart

Abdomen

Back

Physical Examination of hyperaldosteronism

Appearance of the patient

  • Patient is usually well-appearing

Vital signs

Skin

  • There are no abnormal skin findings associated with primary hyperaldosteronism

HEENT

  • HEENT examination is normal in primary hyperaldosteronism.

Neck

Lungs

Heart

Abdomen

  • Non-tender
  • Non-distended
  • No abnormal fluids or gas
  • No palpable organomegaly

Back

  • There are no abnormal findings on the back associated with primary hyperaldosteronism.

Genitourinary

  • There are no abnormal genitourinary findings associated with primary hyperaldosteronism

Extremities

  • Extremities are normal on examination in primary hyperaldosteronism

Neurologic

References

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  2. Bravo EL, Gifford RW (1993). “Pheochromocytoma”. Endocrinol Metab Clin North Am. 22 (2): 329–41. PMID 8325290.
  3. Drénou B, Le Tulzo Y, Caulet-Maugendre S, Le Guerrier A, Leclercq C, Guilhem I; et al. (1995). “Pheochromocytoma and secondary erythrocytosis: role of tumour erythropoietin secretion”. Nouv Rev Fr Hematol. 37 (3): 197–9. PMID 7567437.
  4. La Batide-Alanore A, Chatellier G, Plouin PF (2003). “Diabetes as a marker of pheochromocytoma in hypertensive patients”. J Hypertens. 21 (9): 1703–7. doi:10.1097/01.hjh.0000084729.53355.ce. PMID 12923403.
  5. Kassim TA, Clarke DD, Mai VQ, Clyde PW, Mohamed Shakir KM (2008). “Catecholamine-induced cardiomyopathy”. Endocr Pract. 14 (9): 1137–49. doi:10.4158/EP.14.9.1137. PMID 19158054.
  6. HEINRICH WA, JUDD ES (1948). “A critical analysis of biopsy of lymph nodes”. Proc Staff Meet Mayo Clin. 23 (21): 465–9. PMID 18888946.
  7. Wells SA, Asa SL, Dralle H, Elisei R, Evans DB, Gagel RF; et al. (2015). “Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma”. Thyroid. 25 (6): 567–610. doi:10.1089/thy.2014.0335. PMC 4490627. PMID 25810047.
  8. O’Riordain DS, O’Brien T, Crotty TB, Gharib H, Grant CS, van Heerden JA (1995). “Multiple endocrine neoplasia type 2B: more than an endocrine disorder”. Surgery. 118 (6): 936–42. PMID 7491537.
  9. Wells SA, Asa SL, Dralle H, Elisei R, Evans DB, Gagel RF; et al. (2015). “Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma”. Thyroid. 25 (6): 567–610. doi:10.1089/thy.2014.0335. PMC 4490627. PMID 25810047.
  10. Zelinka T, Holaj R, Petrák O, Strauch B, Kasalický M, Hanus T, Melenovský V, Vancura V, Bürgelová M, Widimský J (2009). “Life-threatening arrhythmia caused by primary aldosteronism”. Med. Sci. Monit. 15 (12): CS174–7. PMID 19946238.
  11. Pella J, Lazúrová I, Javorská B, Trejbal D (1999). “[Conn’s syndrome and severe arrhythmias]”. Vnitr Lek (in Slovak). 45 (4): 228–31. PMID 11045185.
  12. du Cailar G (2004). “[Cardiac consequences of primary hyperaldosteronism]”. Ann Cardiol Angeiol (Paris) (in French). 53 (3): 147–9. PMID 15291171.
  13. Delgado Y, Quesada E, Pérez Arzola M, Bredy R (2006). “Ventricular fibrillation as the first manifestation of primary hyperaldosteronism”. Bol Asoc Med P R. 98 (4): 258–62. PMID 19610566.
  14. Nishimura M, Uzu T, Fujii T, Kuroda S, Nakamura S, Inenaga T, Kimura G (1999). “Cardiovascular complications in patients with primary aldosteronism”. Am. J. Kidney Dis. 33 (2): 261–6. PMID 10023636.

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